OBO ID: DOID:0110711
Term Name: congenital hypotrichosis with juvenile macular dystrophy Search Ontology:
Synonyms:
  • Hjmd
  • hypotrichosis with cone-rod dystrophy
Definition: A hypotrichosis that has_material_basis_in a autosomal recessive mutation of CDH3 on chromosome 16q22.1. https://www.ncbi.nlm.nih.gov/pubmed/11544476
References:
Ontology: Human Disease   (DOID:0110711)
OTHER congenital hypotrichosis with juvenile macular dystrophy PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CDH3 Hypotrichosis, congenital, with juvenile macular dystrophy 601553
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None